A validated single-cell-based strategy to identify diagnostic and therapeutic targets in complex diseases.

Genome Med · 2019 · PMC6664760 · PMID 31358043

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highly significantno p-value reported

We then computed the direct genetic overlaps of all diseases and found them to be highly significant, although the marker with the lowest p value was H3K36me3 (Additional file 3 : Table S4).

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